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高效液相色谱法测定口服红酒后人唾液中的酚类化合物。

Determination of phenolic compounds in human saliva after oral administration of red wine by high performance liquid chromatography.

机构信息

Department of Pharmacy, University of Chieti-Pescara "G. d'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.

Department of Medicine and Aging Sciences, Section of Legal Medicine, University of Chieti-Pescara "G. d'Annunzio", Chieti 66100, Italy.

出版信息

J Pharm Biomed Anal. 2022 Feb 5;209:114486. doi: 10.1016/j.jpba.2021.114486. Epub 2021 Nov 24.

DOI:10.1016/j.jpba.2021.114486
PMID:34847459
Abstract

Red wine is a relevant source of bioactive compounds, which contribute to its antioxidant activity and other beneficial advantages for human health. However, the bioavailability of phenols in humans is not well understood, and the inter-individual variability in the production of phenolic compounds has not been comprehensively assessed to date. The present work describes a new method for the extraction and analysis of phenolic compounds including gallic acid (Gal), vanillic acid (Van), caffeic acid (Caf), syringic acid (Sir); (-)-epicatechin (Epi); p-coumaric acid (Cum) and resveratrol (Rsv) in human saliva samples. The target analytes were extracted using Fabric Phase Sorptive Extraction (FPSE), and subsequently analysed by high-performance liquid chromatography (HPLC) coupled with photodiode array detector (PDA). Chromatographic separation was achieved using a Symmetry C18 RP column in gradient elution mode, with methanol and phosphate buffer as the mobile phases. The linearity (intercept, slope, and determination coefficient) was evaluated in the range from 1 to 50 µg/mL. The limit of quantification (LOQ) was 1 µg/mL (LLOQ ≥0.8 µg/mL), whereas limit of detection was 0.25 µg/mL. The intra and inter-day RSD% and BIAS% values were less than± 15%. The analytical performances were further tested on human saliva collected from healthy volunteers after administering red wine. To the best of our knowledge, this is the first FPSE procedure for the analysis of phenols in saliva, using a non-invasive and easy to perform sample collection protocol. The proposed fast and inexpensive approach can be deployed as a reliable tool to study other biological matrices to proliferate understanding of these compounds distribution in human body.

摘要

红葡萄酒是生物活性化合物的重要来源,这些化合物有助于其抗氧化活性和其他对人类健康的有益优势。然而,人体中酚类物质的生物利用度尚未得到很好的理解,迄今为止也没有全面评估个体间酚类化合物产生的可变性。本工作描述了一种新的方法,用于提取和分析人唾液样本中的酚类化合物,包括没食子酸(Gal)、香草酸(Van)、咖啡酸(Caf)、丁香酸(Sir);(-)-表儿茶素(Epi)、对香豆酸(Cum)和白藜芦醇(Rsv)。目标分析物使用纤维相固相萃取(FPSE)提取,然后通过高效液相色谱(HPLC)与光电二极管阵列检测器(PDA)联用进行分析。采用Symmetry C18 RP 柱在梯度洗脱模式下实现色谱分离,甲醇和磷酸盐缓冲液作为流动相。线性(截距、斜率和决定系数)在 1 至 50 µg/mL 的范围内进行评估。定量下限(LOQ)为 1 µg/mL(LLOQ≥0.8 µg/mL),检测限为 0.25 µg/mL。日内和日间 RSD%和 BIAS%值均小于±15%。在向健康志愿者饮用红葡萄酒后收集的人唾液中进一步测试了分析性能。据我们所知,这是首次使用非侵入性且易于执行的样本采集方案,通过 FPSE 程序分析唾液中的酚类物质。所提出的快速且廉价的方法可以作为一种可靠的工具,用于研究其他生物基质,以加深对这些化合物在人体中分布的理解。

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